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ABOUT ME

My laboratory focuses on two search studies: (1) the pathogenic mechanisms of Alzheimer's disease (AD) and Parkinson’s disease (PD) and (2) development of molecular biomarkers and therapeutic compounds for AD and PD. Upon identification of novel candidate genes from AD and PD patients, we generated primary cultured neurons, patient-derived induced pluripotent stem cells and CRISPR/Cas knockin mice and further study signaling pathways of these genes involved in neurodegeneration. We have earlier identified Ras-Related Protein 35 (RAB35) gene, involved in endocytic recycling, plays an important role in the abnormal α-synuclein protein aggregation in neurons. We further demonstrated that RAB35 promotes the secretion of α-synuclein to extracellular space and causes neuronal death. We generated induced pluripotent stem cells with PLA2G6 mutations and used for studying disease mechanisms. Role and mechanism of PLA2G6 that regulate neuronal is currently under investigation. Further studies are undertaken to examine other molecular mechanisms underlying PD-associated mutations and developed therapeutic strategies for PD.

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EDUCATION

RESEARCH INTERESTS

​Precision medicine of neurodegenerative disease:

Genetic diagnosis for AD and PD.

2005~2009

Ph.D. Chang Gung University, Taiwan

Stem cell therapy:

iPSCs and CRISPR/Cas9 genetic editing

Translational medicine on AD and PD:

Biomarkers 

Therapeutic strategy for AD and PD:  

Small compounds 

2003~2005

M.S. Chang Gung University, Taiwan

1999~2003

B.S. Chung Shan Medical University, Taiwan

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